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Dernières publications
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Francesco Galli, Laricia Bragg, Maira Rossi, Daisy Proietti, Laura Perani, et al.. Cell-mediated exon skipping normalizes dystrophin expression and muscle function in a new mouse model of Duchenne Muscular Dystrophy. EMBO Molecular Medicine, 2024, 16 (4), pp.927 - 944. ⟨10.1038/s44321-024-00031-3⟩. ⟨hal-04603972⟩
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Ekaterina Kiseleva, Olesya Serbina, Anna Karpukhina, Vincent Mouly, Yegor S Vassetzky. Interaction between mesenchymal stem cells and myoblasts in the context of facioscapulohumeral muscular dystrophy contributes to the disease phenotype. Journal of Cellular Physiology, 2022, 237 (8), pp.3328-3337. ⟨10.1002/jcp.30789⟩. ⟨hal-03796151⟩
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Muhammad Haseeb Iqbal, Jeanne Rosine Faratiana, Emeline Pradel, Varvara Gribova, Kamel Mamchaoui, et al.. Brush-Induced Orientation of Collagen Fibers in Layer-by-Layer Nanofilms: A Simple Method for the Development of Human Muscle Fibers. ACS Nano, In press, ⟨10.1021/acsnano.2c06329⟩. ⟨hal-03832239⟩
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Elena Marchesi, Matteo Bovolenta, Lorenzo Preti, Massimo L Capobianco, Kamel Mamchaoui, et al.. Synthesis and Exon-Skipping Properties of a 3′-Ursodeoxycholic Acid-Conjugated Oligonucleotide Targeting DMD Pre-mRNA: Pre-Synthetic versus Post-Synthetic Approach. Molecules, 2021, 26 (24), pp.7662. ⟨10.3390/molecules26247662⟩. ⟨hal-03510261⟩
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Manuel Schmidt, Anja Weidemann, Christine Poser, Anne Bigot, Julia von Maltzahn. Stimulation of Non-canonical NF-κB Through Lymphotoxin-β-Receptor Impairs Myogenic Differentiation and Regeneration of Skeletal Muscle. Frontiers in Cell and Developmental Biology, 2021, 9, ⟨10.3389/fcell.2021.721543⟩. ⟨hal-03405959⟩
Chiffres clés
48
Publications avec texte intégral
Open Access
87 %
Mots clés
Canine X-linked muscular dystrophy in Japan CXMD J
Chromatin
DMD
CXCR4
Fear response
Exondys 51
Gut microbiota
CTG⋅CAGn repeat
Becker muscular dystrophy
Clinical trial candidate screening
Duchenne Muscular Dystrophy
KLF15
Drisapersen
Coculture
MSCs
Myogenesis
Duchenne muscular dystrophy
Machine learning
LTβR
Neuromuscular junction
Fibroblast
Lymphotoxin-β-receptor
Dystrophin
Lamin A/C nuclei
Flavonoid
BAF
Gene Therapy
Developmental biology
Human muscle stem/progenitor cells
Human
Immortalisation
Gene network analysis
Acetylcholine receptor subunit epsilon
DM1 myoblasts
Conjugation
Atrial cardiac defects
CRISPR/Cas9
Folding-defective proteins
Dominant centronuclear myopathy
LRP4
Migration
Muscle
Skeletal muscle
CFTR correctors
Adeno-associated viral vector
BMD
Cell Therapy
Glucose
CMS
3D co-culture
Insulin
ICU-acquired weakness
CLS
Computer software
Expanded repeats
Eteplirsen
FSHD
Mdx
Myotube
Emerin
Glucocorticoid-induced muscle atrophy
Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS
Autophagy
Antisense oligonucleotide
Endocytosis
MT RNA/DNA Editing
Gene therapy
ITSN1
CDNA synthesis
DiPRO1
Fibrosis
Immortalized dystrophic canine myoblast
Lamina-associated domain
Exon-skipping
Adhesion
DNM2
Motor neuron
FoxO
Gel electrophoresis
Exon skipping
Centronuclear myopathy
Alternative splicing
Differentiation
Allele-specific silencing therapy
Cell-penetrating peptide
Cell biology
HDMD/Dmd-null mice
Bile acid
CXCL12
Allele-specific silencing
Exon Skipping
Antisense morpholino
DsDNA break repair
Human artificial chromosomes
Laminographie
Dynamin 2
Myotonic dystrophy
Autophagosome
RNA interference
Actin